OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Raha Pazoki, Marijana Vujković, Joshua Elliott, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 91

Showing 1-25 of 91 citing articles:

Multiomics study of nonalcoholic fatty liver disease
Garðar Sveinbjörnsson, Magnús Ö. Úlfarsson, Rósa B. Þórólfsdóttir, et al.
Nature Genetics (2022) Vol. 54, Iss. 11, pp. 1652-1663
Open Access | Times Cited: 129

Genetic association of lipids and lipid-lowering drug target genes with non-alcoholic fatty liver disease
Ziang Li, Bin Zhang, Qing‐Rong Liu, et al.
EBioMedicine (2023) Vol. 90, pp. 104543-104543
Open Access | Times Cited: 78

Genome-wide characterization of circulating metabolic biomarkers
Minna K. Karjalainen, Savita Karthikeyan, Clare Oliver‐Williams, et al.
Nature (2024) Vol. 628, Iss. 8006, pp. 130-138
Open Access | Times Cited: 75

Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses
Afnan Mansour, Mira Mousa, Dima Abdelmannan, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 48

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Jonas Ghouse, Garðar Sveinbjörnsson, Marijana Vujković, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 827-837
Open Access | Times Cited: 14

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants
Hongbo Liu, Amin Abedini, Eunji Ha, et al.
Science (2025) Vol. 387, Iss. 6734
Closed Access | Times Cited: 1

The individual and global impact of copy-number variants on complex human traits
Chiara Auwerx, Maarja Lepamets, Marie C. Sadler, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 4, pp. 647-668
Open Access | Times Cited: 57

TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
Le Huang, Jonathan D. Rosen, Quan Sun, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 6, pp. 1175-1181
Open Access | Times Cited: 57

The role of obesity, type 2 diabetes, and metabolic factors in gout: A Mendelian randomization study
Yang Yang, Wei Xian, Dide Wu, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 35

Defining type 2 diabetes polygenic risk scores through colocalization and network-based clustering of metabolic trait genetic associations
Samuel Ghatan, Jeroen van Rooij, Mandy van Hoek, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 5

Mapping biological influences on the human plasma proteome beyond the genome
Julia Carrasco-Zanini, Eleanor Wheeler, Burulça Uluvar, et al.
Nature Metabolism (2024)
Open Access | Times Cited: 5

Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder
Joseph D. Deak, Daniel Levey, Frank R. Wendt, et al.
JAMA Network Open (2022) Vol. 5, Iss. 10, pp. e2238880-e2238880
Open Access | Times Cited: 25

Association between antihypertensive drugs and hepatocellular carcinoma: A trans‐ancestry and drug‐target Mendelian randomization study
Zhenqian Wang, Jiawen Lu, Jingyi Hu
Liver International (2023) Vol. 43, Iss. 6, pp. 1320-1331
Closed Access | Times Cited: 13

Associations of liver dysfunction with incident dementia, cognition, and brain structure: A prospective cohort study of 431 699 adults
Pei‐Yang Gao, Ya‐Nan Ou, Hui‐Fu Wang, et al.
Journal of Neurochemistry (2023) Vol. 168, Iss. 1, pp. 26-38
Closed Access | Times Cited: 12

Sex-Hormone-Binding Globulin Gene Polymorphisms and Breast Cancer Risk in Caucasian Women of Russia
Irina Ponomarenko, Konstantin N. Pasenov, Maria Churnosova, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2182-2182
Open Access | Times Cited: 4

Serum liver enzymes and risk of stroke: Systematic review with meta‐analyses and Mendelian randomization studies
Chun Li, Long Gu, Fu‐Yi Shi, et al.
European Journal of Neurology (2024) Vol. 31, Iss. 12
Open Access | Times Cited: 4

A variant in HMMR/HMMR-AS1 is associated with serum alanine aminotransferase levels in the Ryukyu population
Nagaaki Ohyama, Masatoshi Matsunami, Minako Imamura, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access

Evaluating the role of non-alcoholic fatty liver disease in cardiovascular diseases and type 2 diabetes: a Mendelian randomization study in Europeans and East Asians
Shiu Lun Au Yeung, Maria Carolina Borges, Tommy Hon Ting Wong, et al.
International Journal of Epidemiology (2022) Vol. 52, Iss. 3, pp. 921-931
Open Access | Times Cited: 21

Causal impacts of educational attainment on chronic liver diseases and the mediating pathways: Mendelian randomization study
Yiying Wang, Lijie Kong, Chaojie Ye, et al.
Liver International (2023) Vol. 43, Iss. 11, pp. 2379-2392
Closed Access | Times Cited: 11

SparsePro: An efficient fine-mapping method integrating summary statistics and functional annotations
Wenmin Zhang, Hamed S. Najafabadi, Yue Li
PLoS Genetics (2023) Vol. 19, Iss. 12, pp. e1011104-e1011104
Open Access | Times Cited: 11

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